Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/08—Processes
  • C08G18/16—Catalysts
  • C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
  • C08G18/20—Heterocyclic amines; Salts thereof
  • C08G18/2009—Heterocyclic amines; Salts thereof containing one heterocyclic ring
  • C08G18/2027—Heterocyclic amines; Salts thereof containing one heterocyclic ring having two nitrogen atoms in the ring
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/08—Processes
  • C08G18/16—Catalysts
  • C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
  • C08G18/20—Heterocyclic amines; Salts thereof
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G2110/00—Foam properties
  • C08G2110/0008—Foam properties flexible
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G2110/00—Foam properties
  • C08G2110/0083—Foam properties prepared using water as the sole blowing agent

Definitions

• the present invention relates to a process for producing a flexible polyurethane foam through reaction of a polyol and a polyisocyanate in the presence of an amine catalyst, a blowing agent, and a foam stabilizer. More particularly, the present invention relates to a process for producing a flexible polyurethane foam having high air flow from a formulation employing, as the blowing agent, a decreased amount of a halogenated hydrocarbon and an increased amount of water.
• Flexible polyurethane foams are widely used for producing vehicle parts, furniture, bedding, cushions, and the like. Hot mold foams and cold cure mold foams, out of the flexible polyurethane foams, are widely used mainly for seat cushions for automobiles.
• a hot mold foam is produced by mixing a starting liquid formulation for polyurethane composed of a polyisocyanate and a polyol containing an amine catalyst, an organometallic catalyst, a blowing agent, a foam stabilizer, and other auxiliary, then foaming the mixture in a mold kept at 30 to 40°C, post-curing it in an oven, and releasing it from the mold.
• a halogenated hydrocarbon and water are employed as the blowing agent for the hot mold foam.
• a usual formulation for hot mold foams for front backs and rear backs of automobiles employs from 2.0 to 4.5 parts by weight of water and from 5 to 10 parts by weight of a halogenated hydrocarbon such as CFC-11 based on 100 parts by weight of the polyol, as blowing agents.
• a cold cure mold foam which is generally called "HR foam" is produced without conducting post cure in an oven owing to the use of a highly reactive polyol.
• HR foam a halogenated hydrocarbon is used to produce foams of low density and low hardness.
• chlorofluoro carbons such as CFC-11 are indicated to destroy the ozone layer, so that the use of CFCs has come to be regulated and is required to be reduced throughout the world. Consequently, various investigations are being made to develop a formulation employing less CFC-11 and more water instead as the blowing agent in conventional flexible foam formulations. For the same purpose, elevation of the mold temperature up to 50 to 60°C is also being investigated to raise the foaming efficiency.
• a possible method for improving the air flow of the foam is to use, as the amine catalyst, triethylenediamine, bis(dimethylaminoethyl) ether, N-ethylmorpholine, or the like.
• the use of such an amine catalyst narrows the processing latitude, and causes the serious problem of splitting, giving no satisfactory physical properties of the foam.
• an improved formulation for flexible polyurethane foams which contains less CFC-11 and more water as the foaming agent, yet giving high moldability and high air flow.
• the inventors of the present invention made a comprehensive investigation from the above viewpoint regarding the catalyst in the flexible polyurethane foam formulation employing an increased amount of water with a highly reactive polyol having an increased amount of a terminal oxyethylene group, and found that use of an amine having a specific chemical structure as the catalyst enables production of a flexible polyurethane foam having high air flow with improved moldability of the foam.
• the present invention provides a flexible urethane foam formulation which employs an increased amount of water with a highly reactive polyol having an increased amount of terminal oxyethylene groups and yet will give high air flow of the foam with improved moldability.
• the present invention further provides a process for producing a flexible polyurethane foam through reaction of a polyol with a polyisocyanate in the presence of an amine catalyst, a blowing agent, and a foam stabilizer, the amine catalyst comprising at least one of the imidazoles represented by the general formula below: wherein R1 is alkyl of 1 to 4 carbons, dimethylaminopropyl, benzyl, vinyl, or hydroxyalkyl of 1 to 3 carbons; R2 is hydrogen, alkyl of 1 to 4 carbons, allyl, benzyl, or phenyl; and R3 and R4 are respectively hydrogen, alkyl of 1 to 4 carbons, or hydroxymethyl.
• R1 is alkyl of 1 to 4 carbons, dimethylaminopropyl, benzyl, vinyl, or hydroxyalkyl of 1 to 3 carbons
• R2 is hydrogen, alkyl of 1 to 4 carbons, allyl, benzyl, or phenyl
• At least one of the imidazoles represented by the general formula below is employed as a catalyst component wherein R1 is alkyl of 1 to 4 carbons, dimethylaminopropyl, benzyl, vinyl, or hydroxyalkyl of 1 to 3 carbons; R2 is hydrogen, alkyl of 1 to 4 carbons, allyl, benzyl, or phenyl; and R3 and R4 are respectively hydrogen, alkyl of 1 to 4 carbons, or hydroxymethyl.
• the imidazoles in the present invention include specifically 1-methylimidazole, 1,2-dimethylimidazole, 1,4-dimethylimidazole, 1,2,4,5-tetramethylimidazole, 1-methyl-2-ethylimidazole, 1,4-dimethyl-2-ethylimidazole, 1-methyl-2-isopropylimidazole, 1-methyl-2-phenylimidazole, 1-n-butyl-2-methylimidazole, 1-isobutyl-2-methylimidazole, 1-vinylimidazole, 1-benzyl-2-methylimidazole, 1-(3-dimethylaminopropyl)imidazole, and the like.
• 1-methylimidazole 1,2-dimethylimidazole, 1-(3-dimethylaminopropyl)imidazole, 1-n-butyl-2-methylimidazole, and 1-isobutyl-2-methylimidazole, which exhibit high catalytic activity and are highly advantageously utilized in commercial production.
• the catalyst of the present invention may be used combined with another tertiary amine as a cocatalyst.
• the tertiary amine includes triethylamine, N,N-dimethylcyclohexylamine, N,N,N',N'-tetramethylethylenediamine, N,N,N',N'-tetramethylpropylenediamine, N,N,N',N'',N'-pentamethyldiethylenetriamine, N,N,N',N'',N'-pentamethyl-(3-aminopropyl)ethylenediamine, N,N,N',N'',N''-pentamethyldipropylenetriamine, N,N,N',N'-tetramethylguanidine, 1,3,5-tris(N,N-dimethylaminopropyl)hexahydro-s-triazine, 1,8-diazabicyclo 5.4.0 undecene
• tertiary amines preferable are triethylenediamine, N-methyl-N'-(2-dimethylamino)ethylpiperazine, bis(2-dimethylaminoethyl) ether, N-methylmorpholine, and N-ethylmorpholine.
• organic carboxylic acid salts of the aforementioned imidazoles and organic carboxylic acid salts of the aforementioned tertiary amines may properly be used as the catalyst or cocatalyst within the range in which the catalytic function of the present invention is not lost.
• the catalyst of the present invention may be prepared from the above-mentioned imidazole singly or from a mixture of the imidazole and another amine catalyst.
• a solvent such as dipropylene glycol, ethylene glycol, 1,4-butanediol, water, and the like may be used if necessary as the solvent.
• the amount of the solvent is not specially limited, but is preferably not more than 70% of the total amount of the catalyst.
• the catalyst prepared in such a manner may be used by adding it to the polyol.
• Various amine catalysts may be separately added to the polyol.
• the amount of the amine catalyst used in the present invention is generally in the range of from 0.01 to 5.0 parts by weight, preferably from 0.05 to 3.0 parts by weight based on 100 parts by weight of the polyol. If the amount of the amine catalyst used is less than 0.05 parts by weight, the closed cell ratio becomes high and the foam tends to shrink. On the other hand, if the amount of the amine catalyst used is more than 3.0 parts by weight, splitting occurs and the moldability is remarkably impaired.
• the organometallic catalyst includes stannous diacetate, stannous dioctoate, stannous dioleate, stannous dilaurate, dibutyltin oxide, dibutyltin diacetate, dibutyltin dilaurate, dibutyltin dichloride, dioctyltin dilaurate, lead octanoate, lead naphthenate, nickel naphthenate, cobalt naphthenate, and the like.
• organometallic catalysts preferable are organotin catalysts, more preferable are stannous dioctoate, and dibutyltin dilaurate.
• the amount of the organometallic catalyst to be used in the present invention is normally in the range of from 0.01 to 5.0 parts by weight, preferably from 0.05 to 3.0 parts by weight based on 100 parts by weight of the polyol. If the amount of the organometallic catalyst used is not more than 0.05 parts by weight, cracks are liable to develop in the foam. If the amount thereof is not less than 3.0 parts by weight, the foam will shrink.
• the polyol used in the present invention contains at least 5%, preferably 10% by mol of the terminal oxyethylene group in total terminal hydroxyl groups, and having a hydroxyl value in the range of from 10 to 90 mgKOH/g, preferable from 15 to 70 mgKOH/g, although not limited thereto.
• the polyol useful in the present invention includes known polyetherpolyols, polyesterpolyols, and polymer polyols, preferably polyetherpolyols and polymer polyols, and mixtures thereof.
• the polyetherpolyol is prepared by reacting an alkylene oxide such as ethylene oxide and propylene oxide onto a compound having at least two or more active hydrogens such as polyhydric alcohols, e.g., ethylene glycol, propylene glycol, glycerin, trimethylolpropane, pentaerythritol, etc.; amines, e.g., ethylenediamine, etc.; and alkanolamines, e.g., ethanolamine, diethanolamine, etc., for example, according to the method described in "Polyurethane Handbook" (written by Gunther Ortel, Pages 42 - 53).
• the polymer polyols include, for example, reaction products of the aforementioned polyetherpolyol with an ethylenic unsaturated monomer in the presence of a radical polymerization initiator, such as those polymer polyols described in "Polyurethane Handbook" (written by Gunther Ortel, pages 75 and 76).
• the polyisocyanate employed in the present invention may be any of the known organic polyisocyanates, including aromatic polyisocyanates, such as toluene diisocyanate(TDI), 4,4'-diphenylmethane diisocyanate(MDI), naphthylene diisocyanate, xylylene diisocyanate, and the like; aliphatic polyisocyanates such as hexamethylene diisocyanate, and the like; alicyclic polyisocyanates such as dicyclohexyl diisocyanate, isophorone diisocyanate, and the like; and mixtures thereof.
• aromatic polyisocyanates such as toluene diisocyanate(TDI), 4,4'-diphenylmethane diisocyanate(MDI), naphthylene diisocyanate, xylylene diisocyanate, and the like
• aliphatic polyisocyanates such as hexamethylene diisocyan
• TDI and its derivatives include a mixture of 2,4-toluene diisocyanate and 2,6-toluene diisocyanate, and isocyanate-terminated TDI prepolymers.
• the MDI and its derivatives include a mixture of MDI and polyphenyl-polymethylene diisocyanate, namely a polymer of MDI, and/or diphenylmethane diisocyanate derivatives having a terminal isocyanate group.
• the isocyanate index in the present invention is usually in the range of from 70 to 130, although the present invention is not limited to this range.
• the blowing agent useful in the present invention includes water and mixtures of water with a halogenated hydrocarbon.
• the halogenated hydrocarbon includes halogenated methanes and halogenated ethanes such as methylene chloride, trichlorofluoromethane, dichlorodifluoromethane, dichlorotrifluoroethane, and dichloromonofluoroethane.
• the particularly preferred blowing agent is water.
• the amount of water to be used depends on the intended density of the foam, and is usually not less than 2 parts by weight, preferably in the range of from 3.0 to 8.0 parts by weight based on 100 parts by weight of the polyol.
• the foam stabilizer used in the present invention is a conventional organic silicone surfactant, and is used in an amount of from 0.1 to 10 parts by weight based on 100 parts by weight of the polyol.
• a crosslinking agent or a chain extender may be added if necessary.
• the crosslinking agent or the chain extender includes, for example, low molecular-weight polyhydric alcohols such as ethylene glycol, 1,4-butanediol, glycerin, and the like; low molecular-weight aminepolyols such as diethanolamine, triethanolamine, and the like; and polyamines such as ethylenediamine, xylylenediamine, methylene-bis-o-chloroaniline, and the like.
• additives such as a coloring agent, a flame retardant, an age resistor, and the like.
• the kinds and the amount of addition of such additives are used within the usually employed range according to a known procedure.
• the mold temperature at pouring and the oven temperature for post cure are within the range usually employed in known hot mold foam production, and are not specially limited.
• the mold temperature at pouring is in the range of from 30 to 70°C usually, and in the range of from 50 to 70°C in a high mold-temperature process.
• the oven temperature for post cure is in the range of from 150 to 250°C. The foam is cured at this temperature of an oven for 10 to 20 minutes, and is removed from the mold to produce the hot mold foam.
• amine catalyst of the present invention has made it possible to produce foams having high airflow properties from a flexible polyurethane foam formulation employing a decreased amount of a halogenated hydrocarbon and an increased amount of water, which has never readily been achieved. Further, in the hot mold formulation, it has enabled the production of foams having no cracks but improved moldability. Furthermore, with a formulation with an increased amount of organometallic catalyst, or in a process of a high mold-temperature process, it has enabled production of foams having high air permeability and being superior in foam properties.
• the following hot mold foam formulation was employed for the flexible polyurethane foam.
• the foaming tests were conducted by changing the kind of the amine catalyst under predetermined foaming conditions.
• the moldability and the properties of the resulting foams were measured according to the methods shown below. The results are shown in Table 1 and Table 2.
• the density was measured of the test specimen prepared by cutting the central portion of the foam in a size of 20 x 20 x 10 cm.
• the size of splits in the internal portion of the foam was observed, and rated in five grades.

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• 1991
  • 1991-04-05 JP JP3099814A patent/JP3044261B2/ja not_active Expired - Fee Related
  • 1991-04-10 ES ES91105706T patent/ES2074602T5/es not_active Expired - Lifetime
  • 1991-04-10 EP EP91105706A patent/EP0451826B2/fr not_active Expired - Lifetime
  • 1991-04-10 DE DE69111117T patent/DE69111117T3/de not_active Expired - Fee Related
  • 1991-04-11 KR KR1019910005753A patent/KR0182311B1/ko not_active IP Right Cessation
• 1993
  • 1993-02-12 US US08/017,437 patent/US5306738A/en not_active Expired - Lifetime

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